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Analysis of PD-1 related immune transcriptional profile in different cancer types
BACKGROUND: Programmed cell death 1 (PD-1) functions as an immune checkpoint in the process of anti-tumor immune response. The PD-1 blockade is now becoming a fundamental part in cancer immunotherapy. So it’s essential to elicit the PD-1 related immune process in different types of cancer. METHODS:...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307327/ https://www.ncbi.nlm.nih.gov/pubmed/30607140 http://dx.doi.org/10.1186/s12935-018-0712-y |
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author | Shang, Jun Song, Qian Yang, Zuyi Sun, Xiaoyan Xue, Meijuan Chen, Wenjie Yang, Jingcheng Wang, Sihua |
author_facet | Shang, Jun Song, Qian Yang, Zuyi Sun, Xiaoyan Xue, Meijuan Chen, Wenjie Yang, Jingcheng Wang, Sihua |
author_sort | Shang, Jun |
collection | PubMed |
description | BACKGROUND: Programmed cell death 1 (PD-1) functions as an immune checkpoint in the process of anti-tumor immune response. The PD-1 blockade is now becoming a fundamental part in cancer immunotherapy. So it’s essential to elicit the PD-1 related immune process in different types of cancer. METHODS: The Cancer Genome Atlas was used to collect the RNA-seq data of 33 cancer types. The microenvironment cell populations-counter was used to analyze the immune cell infiltrates. KEGG and GO analysis were performed to investigate PD-1 associated biological process. Kaplan–Meier survival curves and Cox’s proportional hazards model were performed for prognostic value analysis. RESULTS: We demonstrated that PD-1 expression varied in different cancer types. The uveal melanoma had a low PD-1 expression and poor infiltrated with immune cells. But it showed the strong correlation of PD-1 with the most types of immune cells. The PD-1 demonstrated a robust relationship with other immunomodulators and showed its involvement in critical functions correlated with anti-tumor immune pathways. Survival analysis indicated the PD-1 expression suggested different prognosis in different cancer types. CONCLUSIONS: Our investigations promote a better understanding of the PD-1 blockade and provide PD-1 related personized combined immunotherapy for different types of cancer patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-018-0712-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6307327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63073272019-01-03 Analysis of PD-1 related immune transcriptional profile in different cancer types Shang, Jun Song, Qian Yang, Zuyi Sun, Xiaoyan Xue, Meijuan Chen, Wenjie Yang, Jingcheng Wang, Sihua Cancer Cell Int Primary Research BACKGROUND: Programmed cell death 1 (PD-1) functions as an immune checkpoint in the process of anti-tumor immune response. The PD-1 blockade is now becoming a fundamental part in cancer immunotherapy. So it’s essential to elicit the PD-1 related immune process in different types of cancer. METHODS: The Cancer Genome Atlas was used to collect the RNA-seq data of 33 cancer types. The microenvironment cell populations-counter was used to analyze the immune cell infiltrates. KEGG and GO analysis were performed to investigate PD-1 associated biological process. Kaplan–Meier survival curves and Cox’s proportional hazards model were performed for prognostic value analysis. RESULTS: We demonstrated that PD-1 expression varied in different cancer types. The uveal melanoma had a low PD-1 expression and poor infiltrated with immune cells. But it showed the strong correlation of PD-1 with the most types of immune cells. The PD-1 demonstrated a robust relationship with other immunomodulators and showed its involvement in critical functions correlated with anti-tumor immune pathways. Survival analysis indicated the PD-1 expression suggested different prognosis in different cancer types. CONCLUSIONS: Our investigations promote a better understanding of the PD-1 blockade and provide PD-1 related personized combined immunotherapy for different types of cancer patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12935-018-0712-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-27 /pmc/articles/PMC6307327/ /pubmed/30607140 http://dx.doi.org/10.1186/s12935-018-0712-y Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Primary Research Shang, Jun Song, Qian Yang, Zuyi Sun, Xiaoyan Xue, Meijuan Chen, Wenjie Yang, Jingcheng Wang, Sihua Analysis of PD-1 related immune transcriptional profile in different cancer types |
title | Analysis of PD-1 related immune transcriptional profile in different cancer types |
title_full | Analysis of PD-1 related immune transcriptional profile in different cancer types |
title_fullStr | Analysis of PD-1 related immune transcriptional profile in different cancer types |
title_full_unstemmed | Analysis of PD-1 related immune transcriptional profile in different cancer types |
title_short | Analysis of PD-1 related immune transcriptional profile in different cancer types |
title_sort | analysis of pd-1 related immune transcriptional profile in different cancer types |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307327/ https://www.ncbi.nlm.nih.gov/pubmed/30607140 http://dx.doi.org/10.1186/s12935-018-0712-y |
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